Yanling Liang

Yanling Liang


Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2020 in Seizure: European Journal of Epilepsy
Verified
Journal Article
Closed access
XFXiaobo Fang
Xiaobo Fang
HWHaibin Wang
Haibin Wang
ZLZifan Liu
Zifan Liu
Jia ChenJia Chen
Jia Chen
HTHu Tan
Hu Tan
DCDunjin Chen
Dunjin Chen

22 September 2021 in Molecular Neurobiology
Verified
Journal Article
Closed access
PDF file
XFXiaobo Fang
Xiaobo Fang
YLYanling Liang
Yanling Liang
WZWei-xi ZHANG
Wei-xi ZHANG
QWQiong Wang
Qiong Wang
JCJingsi Chen
Jingsi Chen
DCDunjin Chen
Dunjin Chen

1 January 2018 in Pregnancy Hypertension
Verified
Journal Article
Closed access
XFXiao-Bo Fang
Xiao-Bo Fang
DCDunjin Chen
Dunjin Chen
FHFang He
Fang He
JCJia Chen
Jia Chen
ZZZhou Zhou
Zhou Zhou
WZWei-xi ZHANG
Wei-xi ZHANG


1 January 2022 in Open Life Sciences
Verified
Journal Article
Open access
PDF file
JCJia Chen
Jia Chen
FHFami Huang
Fami Huang
XFXiaobo Fang
Xiaobo Fang
SLSiying Li
Siying Li
YLYanling Liang
Yanling Liang
The toll-like receptor 4 (TLR4) pathway is involved in seizures. We investigated whether ultrasound-targeted microbubble destruction (UTMD)-mediated delivery of short hairpin RNA (shRNA) targeting the TLR4 gene (shRNA-TLR4) can reduce ischemia-induced seizures in rats with hyperglycemia. A total of 100 male Wistar rats were randomly assigned to five groups: (1) Sham; (2) normal saline (NS); (3) shRNA-TLR4, where rats were injected with shRNA-TLR4; (4) shRNA-TLR4 + US, where rats were injected with shRNA-TLR4 followed by ultrasound (US) irradiation; and (5) shRNA-TLR4 + microbubbles (MBs) + US, where rats were injected with shRNA-TLR4 mixed with MBs followed by US irradiation. Western blot and immunohistochemical staining were used to measure TLR4-positive cells. Half of the rats in the NS group developed tonic-clonic seizures, and TLR4 expression in the CA3 region of the hippocampus was increased in these rats. In addition, the NS group showed an increased number of TLR4-positive cells compared with the Sham group, while there was a decreased number of TLR4-positive cells in the shRNA, shRNA + US, and shRNA + MBs + US groups. Our findings indicate that the TLR4 pathway is involved in the pathogenesis of ischemia-induced seizures in hyperglycemic rats and that UTMD technology may be a promising strategy to treat brain diseases.